Doing community geography     

Fischer  Heather  Block  Daniel  Bosse  Amber  Hawthorne  Timothy L.  Jung  Jin-Kyu  Pearsall  Hamil  Rees  Amanda  Shannon  Jerry 《GeoJournal》2021,87(2):293-306

Community Geography offers researchers, community groups, and students opportunities to engage in action oriented applied geographical research. Creating and sustaining these research programs can be challenging, programs can involve many partners from both academic and the community, have different goals and purposes, and utilize a variety of methods to perform research. In this paper we offer a framework of three primary overarching principles for implementing CG projects; (1) Who, (2) Why, and (3) How. (1) “Who” describes who is involved in CG, including researchers, community partners, academic institutions, (2) “Why” describes the justifications and benefits of taking this approach. (3) “How” explains how CG borrows methodologies from many disciplines within geography and beyond. Our examples are not exhaustive; rather, they serve as starting points to inspire researchers interested in CG.

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Under-ice measurements of suspended particulate matters using ADCP and LISST-Holo     

Ha  Ho Kyung  Kim  Yong Hoon  Lee  Hyun Jung  Hwang  Byongjun  Joo  Hyoung Min 《Ocean Science Journal》2015,50(1):97-108

Ocean Science Journal - Using a mooring package comprising an acoustic Doppler current profiler (ADCP) and holographic imaging system, a 1-day ice camp study was performed under the Arctic sea ice...  相似文献   

The relation between Cu/Au ratio and formation depth of porphyry-style Cu–Au ± Mo deposits     

Hiroyasu Murakami  Jung Hun Seo  Christoph A. Heinrich 《Mineralium Deposita》2010,45(1):11-21

Constraints on gold and copper ore grades in porphyry-style Cu–Au ± Mo deposits are re-examined, with particular emphasis on published fluid pressure and formation depth as indicated by fluid inclusion data and geological reconstruction. Defining an arbitrary subdivision at a molar Cu/Au ratio of 4.0 × 10⁴, copper–gold deposits have a shallower average depth of formation (2.1 km) compared with the average depth of copper–molybdenum deposits (3.7 km), based on assumed lithostatic fluid pressure from microthermometry. The correlation of Cu/Au ratio with depth is primarily influenced by the variations of total Au grade. Despite local mineralogical controls within some ore deposits, the overall Cu/Au ratio of the deposits does not show a significant correlation with the predominant type of Cu–Fe sulfide, i.e., chalcopyrite or bornite. Primary magma source probably contributes to metal endowment on the province scale and in some individual deposits, but does not explain the broad correlation of metal ratios with the pressure of ore formation. By comparison with published experimental and fluid analytical data, the observed correlation of the Cu/Au ratio with fluid pressure can be explained by dominant transport of Cu and Au in a buoyant S-rich vapor, coexisting with minor brine in two-phase magmatic hydrothermal systems. At relatively shallow depth (approximately <3 km), the solubility of both metals decreases rapidly with decreasing density of the ascending vapor plume, forcing both Cu and Au to be coprecipitated. In contrast, magmatic vapor cooling at deeper levels (approximately >3 km) and greater confining pressure is likely to precipitate copper ± molybdenum only, while sulfur-complexed gold remains dissolved in the relatively dense vapor. Upon cooling, this vapor may ultimately contract to a low-salinity epithermal liquid, which can contribute to the formation of epithermal gold deposits several kilometers above the Au-poor porphyry Cu–(Mo) deposit. These findings and interpretations imply that petrographic inspection of fluid inclusion density may be used as an exploration indicator. Low-pressure brine + vapor systems are favorable for coprecipitation of both metals, leading to Au-rich porphyry–copper–gold deposits. Epithermal gold deposits may be associated with such shallow systems, but are likely to derive their ore-forming components from a deeper source, which may include a deeply hidden porphyry–copper ± molybdenum deposit. Exposed high-pressure brine + vapor systems, or stockwork veins containing a single type of intermediate-density inclusions, are more likely to be prospective for porphyry–copper ± molybdenum deposits.  相似文献   

Effects of Resonances in Corrugated Horn Antennas for a 22-GHz Balancing Radiometer     

DeWachter  E. Murk  A. Straub  C. Haefele  A. Soohyun Ka Jung Jin Oh Kampfer  N. 《Geoscience and Remote Sensing Letters, IEEE》2009,6(1):3-7

The Stratospheric WAter vapor RAdiometer (SWARA) is a microwave radiometer designed for ground-based measurements of water vapor (H₂O) in the middle atmosphere (20 to 80 km), including the stratosphere and mesosphere. The instrument is operating in a noncryogenic balancing calibration mode. Since its deployment, features have been observed in the spectrum which can be attributed to resonant variations of the antenna pattern of the corrugated horn. This paper presents copolar and crosspolar antenna pattern measurements of two sister antennas of the SWARA horn, as well as water vapor measurements from both antennas on the ground-based microwave radiometer MI ddle Atmospheric WAter vapor RA diometer. We show that small irregularities in the frequency spectrum at the -20-dB level are visible in the copolar pattern, which, due to the balancing operation scheme used for the radiometer, lead to features in the spectrum that have the same or even higher brightness temperature as the line of interest.  相似文献   

“Amount effect” of water isotopes and quantitative analysis of post‐condensation processes     

Jung‐Eun Lee  Inez Fung 《水文研究》2008,22(1):1-8

A numerical model is proposed that describes the interaction between raindrops and water vapour near the planetary boundary layer to explain the “amount effect”. This model relates the intensity to the isotopic composition of precipitation. The model resolves raindrop sizes, and explicitly includes: (1) the isotopic equilibration time of raindrops that is drop‐size dependent; (2) raindrop transit times through the atmosphere; and (3) the evolution of the isotopic composition of vapour at various rain rates. At high rain rate, the precipitation through a layer is less equilibrated with the vapour because the isotopic equilibration time is long compared to the fast transit time, and there is a preponderance of large drops, which take longer to equilibrate. The δ¹⁸O of vapour in the lower atmosphere becomes lower as a result of the interaction with these raindrops of low δ¹⁸O, and the degree of depletion of ¹⁸O is higher when precipitation rates are high. The model reproduces time‐series observations of isotopic composition of precipitation in Japan, and a vapour replenishment rate is inferred by either advection or evaporation of about 5% of the precipitation rate. The results could be the basis for a new parameterization of the isotopic equilibration for different precipitation types and rates in General Circulation Models (GCMs). When the model is applied to a GCM, this parameterization is important for places where precipitation occurs at cold temperatures (<15 °C). Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

Geochronology in migmatites a SmNd, UPb and RbSr study from the Proterozoic Damara belt (Namibia): implications for polyphase development of migmatites in high-grade terranes     

S. Jung  K. Mezger 《Journal of Metamorphic Geology》2001,19(1):77-97

Sm–Nd (garnet), U–Pb (monazite) and Rb–Sr (biotite) ages from a composite migmatite sample (Damara orogen, Namibia) constrain the time of high‐grade regional metamorphism and the duration of regional metamorphic events. Sm–Nd garnet whole‐rock ages for a strongly restitic melanosome and an adjacent intrusive leucosome yield ages of 534±5, 528±11 and 539±8 Ma. These results provide substantial evidence for pre‐500 Ma Pan‐African regional metamorphism and melting for this segment of the orogen. Other parts of the migmatite yield younger Sm–Nd ages of 488±9 Ma for melanosome and 496±10, 492±5 and 511±16 Ma for the corresponding leucosomes. Garnet from one xenolith from the leucosomes yields an age of 497±2 Ma. Major element compostions of garnet are different in terms of absolute abundances of pyrope and spessartine components, but the flat shape of the elemental patterns suggests late‐stage retrograde equilibration. Rare earth element compositions of the garnet from the different layers are similar except for garnet from the intrusive leucosome suggesting that they grew in different environments. Monazite from the leucosomes is reversely discordant and records ²⁰⁷Pb/²³⁵U ages between 536 and 529 Ma, indicating that this monazite represents incorporated residual material from the first melting event. Monazite from the mesosome MES 2 and the melanosome MEL 3 gives ²⁰⁷Pb/²³⁵U ages of 523 and 526 Ma, and 529 and 531 Ma, respectively, which probably indicates another thermal event. Previously published ²⁰⁷Pb/²³⁵U monazite data give ages between 525 and 521 Ma for composite migmatites, and 521 and 518 Ma for monazite from neosomes. Monazite from granitic to granodioritic veins indicates another thermal event at 507–505 Ma. These ages are also recorded in ²⁰⁷Pb/²³⁵U monazite data of 508 Ma from the metasediment MET 1 from the migmatite and also in the Sm–Nd garnet ages obtained in this study. Taken together, these ages indicate that high‐grade metamorphism started at c. 535 Ma (or earlier) and was followed by thermal events at c. 520 Ma and c. 505 Ma. The latter event is probably connected with the intrusion of a large igneous body (Donkerhoek granite) for which so far only imprecise Rb–Sr whole‐rock data of 520±15 Ma are available. Rb–Sr biotite ages from the different layers of the migmatite are 488, 469 and 473 Ma. These different ages indicate late‐stage disturbance of the Rb–Sr isotopic system on the sub‐sample scale. Nevertheless, these ages are close to the youngest Sm–Nd garnet ages, indicating rapid cooling rates between 13 and 20°C Ma^?1 and fast uplift of this segment of the crust. Similar Sm–Nd garnet and U–Pb monazite ages suggest that the closure temperatures for both isotopic systems are not very different in this case and are probably similar or higher than the previously estimated peak metamorphic temperatures of 730±30°C. The preservation of restitic monazite in leucosomes indicates that dissolution of monazite in felsic water‐undersaturated peraluminous melts can be sluggish. This study shows that geochronological data from migmatites can record polymetamorphic episodes in high‐grade terranes that often contain cryptic evidence for the nature and timing of early metamorphic events.  相似文献   

Processes controlling metal ion attenuation in acid mine drainage streams   总被引：1，自引：0，他引：1  

B.M Chapman  D.R Jones  R.F Jung 《Geochimica et cosmochimica acta》1983,47(11):1957-1973

Two acid mine drainage streams have been investigated by detailed analysis of their sediments and waters, to obtain an understanding of the dominant processes which control the transport and attenuation of heavy metals under conditions of chronic high-level pollutant input. One of the water-courses has a thick hydrous iron oxide crust on its bed, where biotically mediated oxidation of ferrous iron resulted in precipitation of amorphous ferric hydroxide, along with substantial quantities of adsorbed silica, sulphate and Al and lesser quantities of As. Small amounts of K and Pb (and possibly hydronium) jarosites were also present in the sediments. Changes in pH and in the concentrations of Cu, Zn, and Cd appear to be mainly the result of dilution by seeps and tributaries.Although no sediment was recovered during collection of water samples from the second stream, saturation index calculations imply that precipitation should have been occurring. The observed down-stream loss of a number of elements supported this conclusion. The solids predicted to be precipitating were A1(OH)₃, Cu₂(OH)₂CO₃, and Fe(OH)₃. Observed decreases in the concentrations of Cd, Zn and Mn can be accounted for on the basis of dilution alone. However, the additional mechanism of neutralization by higher pH inflows is required to account for the decrease in hydrogen ion concentration downstream.The basis for a potentially useful new technique (congruent element analysis) which enables the identification of conservative components in streams is presented. Comparison of logarithmic concentration versus distance plots delineates the point where chemical removal mechanisms become important for each element.  相似文献   

Hybrid seismic protection of cable‐stayed bridges     

H.‐J. Jung  K.‐S. Park  B. F. Spencer  I.‐W. Lee 《地震工程与结构动力学》2004,33(7):795-820

This paper proposes a hybrid control strategy combining passive and semi‐active control systems for seismic protection of cable‐stayed bridges. The efficacy of this control strategy is verified by examining the ASCE first‐generation benchmark problem for a seismically excited cable‐stayed bridge, which employs a three‐dimensional linearized evaluation bridge model as a testbed structure. Herein, conventional lead–rubber bearings are introduced as base isolation devices, and semi‐active dampers (e.g., variable orifice damper, controllable fluid damper, etc.) are considered as supplemental damping devices. For the semi‐active dampers, a clipped‐optimal control algorithm, shown to perform well in previous studies involving controllable dampers, is considered. Because the semi‐active damper is a controllable energy‐dissipation device that cannot add mechanical energy to the structural system, the proposed hybrid control strategy is fail‐safe in that the bounded‐input, bounded‐output stability of the controlled structure is guaranteed. Numerical simulation results show that the performance of the proposed hybrid control strategy is quite effective in protecting seismically excited cable‐stayed bridges. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

Trace element fractionation during high-grade metamorphism and crustal melting—constraints from ion microprobe data of metapelitic, migmatitic and igneous garnets and implications for Sm–Nd garnet chronology     

S. Jung  E. Hellebrand 《Lithos》2006,87(3-4):193-213

Rare earth element (REE) and other trace element (Y, Sr, Ti, Cr, V, Na) abundances in garnet from a garnet-bearing metapelite, a pelitic migmatite, a syn-tectonic granite and a post-tectonic leucogranite were measured by secondary ion mass spectrometry (SIMS) in order to identify the effective variables on the trace element distribution between garnet and the host rock. Garnet from the garnet-bearing metapelite, the pelitic migmatite and the syn-tectonic granite is zoned with respect to REE. The cores are enriched by a factor of 2–3 relative to the rims. For the garnets from the garnet-bearing metapelite equilibrium distribution following a simple Rayleigh fractionation is responsible for the decreasing concentrations in REE from core to rim. Garnet from the pelitic migmatite shows a more complex trace element pattern following distinct enrichment and depletion patterns for Ti, V, Cr and REE from core to rim. These features suggest disequilibrium between garnet and the associated melt in which the enrichment of trace elements probably correspond to a period of open-system behaviour in these rocks at a time when the garnet, originally nucleated in the metamorphic environment was incorporated into the melt. The garnet from the syn-tectonic granite shows stepwise decreasing concentrations in REE from core to rim: a REE-rich core can be distinguished from a broad REE-depleted rim. Notably, from core to rim an inflection of the Yb / Er and Yb / Dy ratios is visible. Whereas the decrease of HREE abundance in the core region of the garnet from the syn-tectonic granite may arise from equilibrium partitioning during garnet growth, the inflection can be interpreted as a result of partial melting. Garnet cores with high Yb / Er and Yb / Dy >  1 nucleated in the metamorphic environment without the presence of a melt whereas the rims with lower Yb / Er and Yb / Dy <  1 crystallized in the presence of a melt. Garnet from the leucogranite has lower REE abundances and is considered to be of igneous origin. In contrast to garnet from the other samples, its core has low trace element abundances, whereas its rim is significantly enriched in REE but depleted in Ti. These features suggest that only the outermost rim was in equilibrium with the melt. For this garnet, liquid diffusion controlled partitioning is more likely to explain the extreme trace element variation. An evaluation of Sm and Nd concentrations in garnet and a comparison of Sm–Nd and U–Pb garnet ages and U–Pb monazite ages form the terrane indicate that the observed LREE systematics in the different garnet species are a primary feature and are not homogenized by volume diffusion during high grade amphibolite facies conditions.  相似文献   

Microbial effects on geochemical behavior of arsenic in As-contaminated sediments   总被引：4，自引：0，他引：4  

J.M. Park  J.S. Lee  J.-U. Lee  H.T. Chon  M.C. Jung 《Journal of Geochemical Exploration》2006,88(1-3):134

The purpose of this study is to investigate the contamination level and chemical speciation of As in sediments from the Hwachon Au mine area, and to study the effects of indigenous bacteria on geochemical behavior of As in As-contaminated sediments from the mine. Concentrations of heavy metal and metalloids in one composite sample of 9 Hwachon sediments were 24.9 As mg/kg, 16.6 Cd mg/kg, 230 Pb mg/kg and 1080 Zn mg/kg. This indicates that this area was seriously contaminated with As, Cd and Zn. From the result of sequential extraction analysis, most of As (87.9%) existed as a phase of As which coprecipitated with Fe oxyhydroxides. Under aerobic condition, As concentration leached from sediments were 4 times higher in non-sterile than in sterile condition. This enrichment of As leaching could be caused by increase of pH and exudation secreted during microbial metabolism. On the other hand, under anaerobic condition, As concentration has dramatically increased in non-sterile solution with time. This As leaching has begun on 4–5th days of incubation and the highest concentration of 511 As μg/l was recorded on about 11th day. Arsenic leaching under anaerobic condition was caused by microbial enhancement of Fe leaching. Total Fe concentration increased from the 4th day, and this Fe leaching might cause lixiviation of As which had been coprecipitated with Fe oxyhydroxide.  相似文献